A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034782



Internal ID21944125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63730020..63730113hg38UCSC Ensembl
chr17:61807380..61807473hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624500
Samples
Known GenesSTRADA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034782
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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